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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 2
1983 2
1985 1
1986 1
1987 4
1990 1
1991 1
1993 1
1995 2
1998 2
2000 3
2001 1
2003 2
2005 3
2006 3
2007 1
2008 4
2010 1
2011 4
2012 3
2013 3
2014 3
2015 5
2016 3
2017 4
2018 3
2019 4
2020 2
2022 5
2023 2
2024 3

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71 results

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Page 1
Flow cytometry-based diagnosis of primary immunodeficiency diseases.
Kanegane H, Hoshino A, Okano T, Yasumi T, Wada T, Takada H, Okada S, Yamashita M, Yeh TW, Nishikomori R, Takagi M, Imai K, Ochs HD, Morio T. Kanegane H, et al. Allergol Int. 2018 Jan;67(1):43-54. doi: 10.1016/j.alit.2017.06.003. Epub 2017 Jul 3. Allergol Int. 2018. PMID: 28684198 Free article. Review.
Flow cytometry effectively identifies major forms of PIDs, including severe combined immunodeficiency, X-linked agammaglobulinemia, hyper IgM syndromes, Wiskott-Aldrich syndrome, X-linked lymphoproliferative syndrome, familial hemophagocytic lymphohist …
Flow cytometry effectively identifies major forms of PIDs, including severe combined immunodeficiency, X-linked agammaglobulinemia, hyper Ig …
Genomic diagnosis and care co-ordination for monogenic inflammatory bowel disease in children and adults: consensus guideline on behalf of the British Society of Gastroenterology and British Society of Paediatric Gastroenterology, Hepatology and Nutrition.
Kammermeier J, Lamb CA, Jones KDJ, Anderson CA, Baple EL, Bolton C, Braggins H, Coulter TI, Gilmour KC, Gregory V, Hambleton S, Hartley D, Hawthorne AB, Hearn S, Laurence A, Parkes M, Russell RK, Speight RA, Travis S, Wilson DC, Uhlig HH. Kammermeier J, et al. Lancet Gastroenterol Hepatol. 2023 Mar;8(3):271-286. doi: 10.1016/S2468-1253(22)00337-5. Epub 2023 Jan 9. Lancet Gastroenterol Hepatol. 2023. PMID: 36634696 Review.
X-linked lymphoproliferative syndrome.
Nelson DL, Terhorst C. Nelson DL, et al. Clin Exp Immunol. 2000 Dec;122(3):291-5. doi: 10.1046/j.1365-2249.2000.01400.x. Clin Exp Immunol. 2000. PMID: 11122230 Free PMC article. Review. No abstract available.
Rare diseases presenting with hemophagocytic lymphohistiocytosis.
Kanegane H, Noguchi A, Yamada Y, Yasumi T. Kanegane H, et al. Pediatr Int. 2023 Jan-Dec;65(1):e15516. doi: 10.1111/ped.15516. Pediatr Int. 2023. PMID: 36843347 Review.
HLH is caused by a variety of factors and is classified into primary and secondary HLH. Familial HLH (FHL) types 1-5, X-linked lymphoproliferative syndrome types 1 and 2, and FHL syndrome with hypopigmentation are all examples of primary HLH. ...
HLH is caused by a variety of factors and is classified into primary and secondary HLH. Familial HLH (FHL) types 1-5, X-linked …
Pathogenesis and diagnosis of X-linked lymphoproliferative disease.
Gilmour KC, Gaspar HB. Gilmour KC, et al. Expert Rev Mol Diagn. 2003 Sep;3(5):549-61. doi: 10.1586/14737159.3.5.549. Expert Rev Mol Diagn. 2003. PMID: 14510176 Review.
X-linked lymphoproliferative syndrome (XLP) is a rare, often fatal, primary immunodeficiency that has profound and damaging effects on the immune system of affected individuals. ...
X-linked lymphoproliferative syndrome (XLP) is a rare, often fatal, primary immunodeficiency that has profound a …
X-linked inhibitor of apoptosis protein deficiency: more than an X-linked lymphoproliferative syndrome.
Aguilar C, Latour S. Aguilar C, et al. J Clin Immunol. 2015 May;35(4):331-8. doi: 10.1007/s10875-015-0141-9. Epub 2015 Mar 4. J Clin Immunol. 2015. PMID: 25737324 Review.
X-linked inhibitor of apoptosis (XIAP) deficiency (also known as X-linked lymphoproliferative syndrome type 2, XLP-2) is a rare primary immunodeficiency. ...
X-linked inhibitor of apoptosis (XIAP) deficiency (also known as X-linked lymphoproliferative syndrome type 2, X …
X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic.
Xu T, Zhao Q, Li W, Chen X, Xue X, Chen Z, Du X, Bai X, Zhao Q, Zhou L, Tang X, Yang X, Kanegane H, Zhao X. Xu T, et al. Eur J Pediatr. 2020 Feb;179(2):327-338. doi: 10.1007/s00431-019-03512-7. Epub 2019 Nov 21. Eur J Pediatr. 2020. PMID: 31754776 Free PMC article.
X-linked lymphoproliferative syndrome (XLP) is a rare primary immunodeficiency disease that can be divided into two types: SAP deficiency (XLP1) and XIAP deficiency (XLP2), caused by mutations in the SH2D1A and XIAP genes, respectively. ...
X-linked lymphoproliferative syndrome (XLP) is a rare primary immunodeficiency disease that can be divided into …
X-Linked Lymphoproliferative Syndrome Presenting as Adult-Onset Multi-Infarct Dementia.
Blackburn PR, Lin WL, Miller DA, Lorenzo-Betancor O, Edwards ES, Zimmermann MT, Farrugia LP, Freeman WD, Soto AI, Walton RL, Klee EW, Atwal PS, Abraham RS, Billadeau DD, Ross OA, Dickson DW, Meschia JF. Blackburn PR, et al. J Neuropathol Exp Neurol. 2019 May 1;78(5):460-466. doi: 10.1093/jnen/nlz018. J Neuropathol Exp Neurol. 2019. PMID: 30990878 Free PMC article.
Novel immunodeficiency data servers.
Väliaho J, Riikonen P, Vihinen M. Väliaho J, et al. Immunol Rev. 2000 Dec;178:177-85. doi: 10.1034/j.1600-065x.2000.17807.x. Immunol Rev. 2000. PMID: 11213802 Review.
Currently 14 registries are distributed, including information about Bloom syndrome (BLMbase), X-linked agammaglobulinemia (BTKbase), X-linked and autosomal recessive chronic granulomatous diseases (CYBBbase for X-linked CGD, CYBAbase for p22(phox) deficiency, NCF1base for p47(ph …
Currently 14 registries are distributed, including information about Bloom syndrome (BLMbase), X-linked agammaglobulinemia (BTKbase), X-link …
Prenatal diagnosis and genetic analysis of X-linked immunodeficiency disorders.
Puck JM. Puck JM. Pediatr Res. 1993 Jan;33(1 Suppl):S29-33; discussion S33-4. doi: 10.1203/00006450-199305001-00158. Pediatr Res. 1993. PMID: 8433872 Review.
Several congenital immunodeficiency diseases can exhibit X-linked inheritance, including agammaglobulinemia, severe combined immunodeficiency, Wiskott-Aldrich syndrome, X-linked lymphoproliferative syndrome, and X-linked hyper-IgM syndrome. ...
Several congenital immunodeficiency diseases can exhibit X-linked inheritance, including agammaglobulinemia, severe combined immunodeficienc …
71 results